2-(2-azidomethyl-4-methoxy-phenyl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide

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Chemical Name:2-(2-azidomethyl-4-methoxy-phenyl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide
CAS No.:228259-24-3
Molecular Formula:C₂₉H₂₈F₃N₇O₄S
Molecular Weight:627.647
Hs Code.:

2-(2-azidomethyl-4-methoxy-phenyl)-5-trifluoromethyl-2<i>H</i>-pyrazole-3-carboxylic acid (2'-<i>tert</i>-butylsulfamoyl-biphenyl-4-yl)-amide

Synonyms:2-(2-azidomethyl-4-methoxy-phenyl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide

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Chemical Property of 2-(2-azidomethyl-4-methoxy-phenyl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide

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Technology Process of 2-(2-azidomethyl-4-methoxy-phenyl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide

There total 10 articles about 2-(2-azidomethyl-4-methoxy-phenyl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 193006-34-7
4-(2'-tert-butylaminosulfonylphenyl)aniline

: 228259-19-6
1-(2-azidomethyl-4-methoxyphenyl)-3-trifluoromethyl-1H-pyrazole-5-carboxylic acid chloride

: 228259-24-3
2-(2-azidomethyl-4-methoxy-phenyl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide

Guidance literature:: With pyridine; dmap; In dichloromethane; at 20 ℃;
DOI:10.1021/jm030212h

Reference yield:

: 326-90-9
4,4,4-trifluoro-1-(2-furanyl)-1,3-butanedione

: 228259-24-3
2-(2-azidomethyl-4-methoxy-phenyl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide

Guidance literature:: Multi-step reaction with 8 steps

1: AcOH / 4 h / 100 °C

2: N-methylmorpholine / tetrahydrofuran / 0.5 h / 0 °C

3: 1.5 g / NaBH₄ / tetrahydrofuran; H₂O

4: Et₃N / CHCl₃ / 4 h / cooling

5: 1.43 g / NaN₃ / dimethylformamide / 2 h / 60 °C

6: 68 percent / potassium permanganate / acetone; H₂O / 3 h / 60 °C

7: oxalyl chloride; DMF / CH₂Cl₂ / 3 h / 0 °C

8: pyridine; DMAP / CH₂Cl₂ / 20 °C

With 4-methyl-morpholine; pyridine; dmap; sodium tetrahydroborate; potassium permanganate; sodium azide; oxalyl dichloride; acetic acid; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane; chloroform; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm030212h

Reference yield:

: 6705-03-9
2-Amino-5-methoxybenzoic acid

: 228259-24-3
2-(2-azidomethyl-4-methoxy-phenyl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (2'-tert-butylsulfamoyl-biphenyl-4-yl)-amide

Guidance literature:: Multi-step reaction with 9 steps

1.1: HCl; NaNO₂ / H₂O / 0.5 h / 0 °C

1.2: SnCl₂*2H₂O; HCl / H₂O / 3 h / 0 - 20 °C

2.1: AcOH / 4 h / 100 °C

3.1: N-methylmorpholine / tetrahydrofuran / 0.5 h / 0 °C

4.1: 1.5 g / NaBH₄ / tetrahydrofuran; H₂O

5.1: Et₃N / CHCl₃ / 4 h / cooling

6.1: 1.43 g / NaN₃ / dimethylformamide / 2 h / 60 °C

7.1: 68 percent / potassium permanganate / acetone; H₂O / 3 h / 60 °C

8.1: oxalyl chloride; DMF / CH₂Cl₂ / 3 h / 0 °C

9.1: pyridine; DMAP / CH₂Cl₂ / 20 °C

With 4-methyl-morpholine; pyridine; hydrogenchloride; dmap; sodium tetrahydroborate; potassium permanganate; sodium azide; oxalyl dichloride; acetic acid; triethylamine; N,N-dimethyl-formamide; sodium nitrite; In tetrahydrofuran; dichloromethane; chloroform; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm030212h